Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K120676 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
MEVION S250 Product Usage: Proton Radiation Therapy System | 2 | 11/15/2016 | Mevion Medical Systems, Inc. |
MEVION S250 Product Usage: Proton Radiation Therapy | 2 | 11/15/2016 | Mevion Medical Systems, Inc. |
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